Canonical Allele Identifier: CA394823554
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs2141620707

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948004G>C , CM000678.2:g.13948004G>C GRCh38
NC_000016.9:g.14041861G>C , CM000678.1:g.14041861G>C GRCh37
NC_000016.8:g.13949362G>C NCBI36
NG_011442.1:g.32848G>C , LRG_463:g.32848G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2546G>C ENSP00000507912.1:p.Cys849Ser
ENST00000683962.1:c.*2102G>C ENSP00000506854.1:n.*2102G>C
ENST00000311895.8:c.2408G>C MANE Select ENSP00000310520.7:p.Cys803Ser
ENST00000311895.7:c.2408G>C ENSP00000310520.7:p.Cys803Ser
ENST00000389138.7:n.1685G>C
ENST00000462862.1:c.721G>C ENSP00000461322.1:n.721G>C
NM_005236.2:c.2408G>C , LRG_463t1:c.2408G>C NP_005227.1:p.Cys803Ser
XM_011522424.1:c.2546G>C XP_011520726.1:p.Cys849Ser
XM_011522425.1:c.1865G>C XP_011520727.1:p.Cys622Ser
XM_011522426.1:c.1619G>C XP_011520728.1:p.Cys540Ser
XM_011522427.1:c.1058G>C XP_011520729.1:p.Cys353Ser
XR_932805.1:n.2567G>C
XM_011522424.3:c.2546G>C XP_011520726.1:p.Cys849Ser
XM_017023043.2:c.1619G>C XP_016878532.1:p.Cys540Ser
NM_005236.3:c.2408G>C MANE Select NP_005227.1:p.Cys803Ser